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Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
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Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
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Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation

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Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation
Journal Article

Biofunctional Polyacrylamide Hydrogels using Tetrazole‐Methylsulfone Comonomer for Thiol Conjugation

2024
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Overview
Biofunctionalized polyacrylamide (PAAm) hydrogels are important 2D substrates for studying cell physics and mechanobiology. In this work, an arylmethylsulfone (MS) comonomer is developed that can be incorporated into PAAm gels under aqueous radical polymerization conditions. The resulting hydrogels show similar properties to unmodified PAAm gels, indicating that the comonomer is incorporated without affecting PAAm physical properties. The MS‐containing PAAm hydrogels allow efficient conjugation of thiol derivatized biomolecules and require very low comonomer content (2 mM, 0.18 mol% relative to AAm) and thiol incubation amounts (≥ 0.15 µg per gel) to achieve functional densities that elicit cell responses. Compared to carboxyl‐functionalized PAAm hydrogels, a 10‐fold lower comonomer concentration and a 10‐fold lower ligand feed concentration are sufficient to achieve comparable cell adhesion responses. The new comonomer opens up possibilities for efficient and straightforward biofunctionalization of PAAm hydrogels used in cell biophysical studies. A new methylsulfone comonomer is presented that can be integrated into polyacrylamide hydrogels for efficient biofunctionalization with thiol‐bearing ligands. Very low comonomer and ligand incubation amounts are required to achieve ligand densities that elicit cell responses, offering an efficient pathway to bioactive hydrogel surfaces for cell physics and mechanobiology studies.